Correction to: Nature Communications https://doi.org/10.1038/s41467-018-06014-6, published online 05 November 2018.
The HTML and PDF versions of this Article were updated after publication to remove images of one individual from Fig. 1.
Author information
These authors contributed equally: Lot Snijders Blok, Justine Rousseau, Joanna Twist.
These authors jointly supervised this work: Simon E. Fisher, Philippe M. Campeau.
Authors and Affiliations
Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands
Lot Snijders Blok, Stefan Lelieveld, Rolph Pfundt, Sandra Jansen, Tjitske Kleefstra & Han G. Brunner
Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands
Lot Snijders Blok, Pelagia Deriziotis & Simon E. Fisher
Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands
Lot Snijders Blok, Sandra Jansen, Tjitske Kleefstra, Han G. Brunner & Simon E. Fisher
CHU Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada
Justine Rousseau, Sophie Ehresmann & Philippe M. Campeau
National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA
Joanna Twist, Motoki Takaku, Cat Taylor, John D. Roberts, Robert M. Petrovich & Paul A. Wade
Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands
Hanka Venselaar
Division of Genetics and Genomics, Boston Children’s Hospital, Boston, MA 02115, USA
Lance H. Rodan, Catherine B. Nowak & Jessica Douglas
Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA
Kathryn J. Swoboda
Department of Medical Genetics, Massachusetts General Hospital, Boston, MA 02114, USA
Marcie A. Steeves & Inderneel Sahai
Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands
Connie T. R. M. Stumpel, Alexander P. A. Stegmann & Han G. Brunner
Nemours Childrens Clinic, Orlando, FL 32827, USA
Patricia Wheeler
Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA
Marcia Willing & Elise Fiala
Valley Children’s Hospital, Madera, CA 93636, USA
Aaina Kochhar
British Columbia Children’s Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada
William T. Gibson, Ana S. A. Cohen & Ruky Agbahovbe
Department of Medical Genetics, University of British Columbia, Vancouver, BC V6H 3N1, Canada
William T. Gibson, Ana S. A. Cohen & Ruky Agbahovbe
Department of Medical Genetics and Alberta Children’s Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada
A. Micheil Innes & P. Y. Billie Au
Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree), Exeter, EX2 5DW, UK
Julia Rankin
Division of Genetics, Department of Medicine, University of Tennessee Medical Center, Knoxville, TN 37920, USA
Ilse J. Anderson
Greenwood Genetic Center, Greenwood, SC 29646, USA
Steven A. Skinner, Raymond J. Louie & Hannah E. Warren
GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris ; Department of Medical Genetics and Centre de Référence Malformations et maladies congénitales du cervelet et déficiences intellectuelles de causes rares, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France
Alexandra Afenjar
AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France
Boris Keren, Caroline Nava & Julien Buratti
Groupe de Recherche Clinique (GRC) ‘déficience intellectuelle et autisme’ UPMC, Paris, 75005, France
Boris Keren & Caroline Nava
INSERM, U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, 75013, Paris, France
Caroline Nava
GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department Child Neurology and Reference Center for Neuromuscular Diseases “Nord/Est/Ile-de-France”, FILNEMUS, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France
Arnaud Isapof
GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department of Child Neurology and National Reference Center for Neurogenetic Disorders, Armand Trousseau Hospital, GHUEP, AP-HP, INSERM U1141, 75012, Paris, France
Diana Rodriguez
Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA 23298, USA
Raymond Lewandowski & Jennifer Propst
Clinical Genetics Department, University Medical Center Groningen, Groningen, 9700RB, The Netherlands
Ton van Essen
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea
Murim Choi & Sangmoon Lee
Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children’s Hospital, Seoul, 08826, Republic of Korea
Jong H. Chae
Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 7HE, UK
Susan Price
GeneDx, Gaithersburg, MD 20877, USA
Rhonda E. Schnur, Ganka Douglas & Ingrid M. Wentzensen
Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany
Christiane Zweier & André Reis
Northwell Health, Division of Medical Genetics and Genomics, Great Neck, NY 11021, USA
Martin G. Bialer & Christine Moore
Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands
Marije Koopmans, Eva H. Brilstra, Glen R. Monroe, Koen L. I. van Gassen & Ellen van Binsbergen
University Hospitals Bristol, Department of Clinical Genetics, St Michael’s Hospital, Bristol, BS2 8EG, UK
Ruth Newbury-Ecob & Lucy Bownass
Department of Clinical Genetics, University Children’s Hospital, Paracelsus Medical University, Salzburg, A-5020, Austria
Ingrid Bader
Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria
Johannes A. Mayr & Saskia B. Wortmann
Institute of Human Genetics, Technische Universität München, Munich, 81675, Germany
Saskia B. Wortmann
Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, 85764, Germany
Saskia B. Wortmann
Communication Sciences and Disorders, Augustana College, Rock Island, IL 61201, USA
Kathy J. Jakielski
Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA
Edythe A. Strand
Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany
Katja Kloth & Tatjana Bierhals
Waseda University, Tokyo, 169-8050, Japan
Shinichi Machida & Hitoshi Kurumizaka
Equipe Génétique des Anomalies du Développement, Université de Bourgogne-Franche Comté, Dijon, 21070, France
Laurence Faivre, Julien Thevenon & Mirna Assoum
Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d’Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France
Laurence Faivre, Julien Thevenon & Mirna Assoum
Waisman Center, Phonology Project, Madison, WI 53705-2280, USA
Lawrence Shriberg
Sainte-Justine Hospital, University of Montreal, Montreal, QC H3T 1C5, Canada
Philippe M. Campeau
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK
Jeremy F. McRae, Stephen Clayton, Tomas W. Fitzgerald, Joanna Kaplanis, Elena Prigmore, Diana Rajan, Alejandro Sifrim, Nadia Akawi, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, Philip Jones, Wendy D. Jones, Daniel King, Netravathi Krishnappa, Laura E. Mason, Tarjinder Singh, Adrian R. Tivey, Jana Awada, A. Paul Bevan, Simon Brent, Elena Chatzimichali, Irina Colgiu, Dylan de Vries, Emma Gray, Philip Greene, Susan Gribble, Liu He, Lucy Hildyard, Ben Hutton, Rosemary Kelsell, Anna Middleton, Daniel Perrett, Martin Pollard, Raheleh Rahbari, Josh Randall, Ganesh Jawahar Swaminathan, Parthiban Vijayarangakannan, Sara Widaa, Emily Wilkinson, Helen V. Firth, Caroline F. Wright, David R. FitzPatrick, Jeffrey C. Barrett & Matthew E. Hurles
MRC Human Genetics Unit, MRC IGMM, University of Edinburgh, Western General Hospital, Edinburgh, EH4 2XU, UK
Stuart Aitken, Andrew Jackson, Wayne Lam, Anne Lampe, Eddy Maher, David Moore & David R. FitzPatrick
Department of Engineering Science, University of Oxford, Parks Road, Oxford, OX1 3PJ, UK
Mohsan Alvi
Wessex Clinical Genetics Service, University Hospital Southampton, Princess Anne Hospital, Coxford Road, Southampton, SO16 5YA, UK
Munaza Ahmed, Diana Baralle, David J. Bunyan, Amanda Collins, Morag N. Collinson, Nicola Foulds, Lucy Harrison, Victoria Harrison, Katherine Lachlan, I. Karen Temple, Audrey Torokwa & Diana Wellesley
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Faculty of Medicine, University of Southampton, Building 85, Life Sciences Building, Highfield Campus, Southampton, SO17 1BJ, UK
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Manchester Centre for Genomic Medicine, St Mary’s Hospital, Central Manchester University Hospitals NHSFoundation Trust, Manchester Academic Health Science Centre, Manchester, M13 9WL, UK
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Nuffield Department of Obstetrics & Gynaecology, University of Oxford, Level 3, Women’s Centre, John Radcliffe Hospital, Oxford, OX3 9DU, UK
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Correspondence to Simon E. Fisher or Philippe M. Campeau.
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Snijders Blok, L., Rousseau, J., Twist, J. et al. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nat Commun 10, 2079 (2019). https://doi.org/10.1038/s41467-019-10161-9
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DOI: https://doi.org/10.1038/s41467-019-10161-9
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